Department of Biochemistry, College of Medicine and Medical Sciences (CMMS), Arabian Gulf University (AGU), Manama, Bahrain; Farwaniya Hospital, Biochemistry Laboratory, PO Box 13373, Farwaniya 81004, Kuwait.
Department of Biological Sciences, Faculty of Science, Kuwait University, Kuwait City, Kuwait.
Gene. 2021 Jan 15;766:145127. doi: 10.1016/j.gene.2020.145127. Epub 2020 Sep 13.
Telomeres are duplex tandem repeats of DNA sequence 5'-TTAGGG-3' at chromosomal ends synthesized by telomerase enzyme (TE). Telomeres length (TL) shortening is associated with age and age-related disorders. Recently, we demonstrated marked leukocytes TL (LTL) shortening in T2DM. To set the relationship between the TE, LTL and T2DM, we analyzed samples from 212 Kuwaiti subjects, 112 patients withT2DM and 100 non-diabetic subjects. The plasma TE and fasting insulin were measured by ELISA, the LTL was estimated by qPCR and three SNPs of genes related to TL; TERC rs12696304 (C/G), TERT rs2736100 (C/A) and ACYP2 rs6713088 (C/G) were genotyped by rtPCR. Results revealed comparable TE levels and alleles/genotypes between the cases and controls with no influence of either on the LTL. Interestingly, although the plasma concentration of the TE was generally low, it was significantly influenced by the TERT and ACYP2 but not TERC polymorphisms. The CC genotype carriers of rs2736100 (C/A) had significantly higher plasma TE levels compared to CA and AA carriers, p 0.009 and p 0.047, respectively, and the A-allele was associated with low TE, p 0.018. Similarly, significantly higher TE levels were detected in CC carriers of ACYP2 rs6713088 (C/G) compared with GC carriers, p 0.002, and the G-allele was associated with low TE, p 0.009. Finally, the TERT and ACYP2 polymorphisms had an influence on blood glucose levels. In conclusion, the telomeres shortening in T2DM was not due to TE deficiency or gene polymorphisms, while the TE levels were significantly associated with the TERT and ACYP2 but not TERC polymorphisms.
端粒是染色体末端由端粒酶(TE)合成的 DNA 序列 5'-TTAGGG-3'的双链串联重复。端粒长度(TL)缩短与年龄和与年龄相关的疾病有关。最近,我们在 T2DM 中发现明显的白细胞 TL(LTL)缩短。为了确定 TE、LTL 和 T2DM 之间的关系,我们分析了来自 212 名科威特受试者的样本,其中 112 名患者患有 T2DM,100 名非糖尿病患者。通过 ELISA 测量血浆 TE 和空腹胰岛素,通过 qPCR 估计 LTL,并通过 rtPCR 对与 TL 相关的三个基因的 SNPs;TERC rs12696304(C/G)、TERT rs2736100(C/A)和 ACYP2 rs6713088(C/G)进行基因分型。结果表明,病例组和对照组的 TE 水平和等位基因/基因型相当,LTL 不受影响。有趣的是,尽管 TE 的血浆浓度通常较低,但它受到 TERT 和 ACYP2 的显著影响,但不受 TERC 多态性的影响。rs2736100(C/A)的 CC 基因型携带者的血浆 TE 水平明显高于 CA 和 AA 携带者,p 0.009 和 p 0.047,A 等位基因与低 TE 相关,p 0.018。同样,ACYP2 rs6713088(C/G)的 CC 携带者的 TE 水平明显高于 GC 携带者,p 0.002,G 等位基因与低 TE 相关,p 0.009。最后,TERT 和 ACYP2 多态性对血糖水平有影响。总之,T2DM 中的端粒缩短不是由于 TE 缺乏或基因多态性引起的,而 TE 水平与 TERT 和 ACYP2 显著相关,但与 TERC 多态性无关。